Iron(III) pyrophosphate

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Iron(III) pyrophosphate
Iron(III) pyrophosphate.svg
Names
Other names
Ferric pyrophosphate
Identifiers
  • 10058-44-3(anhydrous) Yes check.svgY
  • 10049-18-0(nonahydrate) Yes check.svgY
3D model (JSmol)
ChEBI
ChemSpider
DrugBank
ECHA InfoCard 100.030.160 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 233-190-0
PubChem CID
UNII
  • Key: CADNYOZXMIKYPR-UHFFFAOYSA-B
  • InChI=1S/4Fe.3H4O7P2/c;;;;3*1-8(2,3)7-9(4,5)6/h;;;;3*(H2,1,2,3)(H2,4,5,6)/q4*+3;;;/p-12
  • [Fe+3].O=P([O-])([O-])OP(=O)([O-])[O-].[Fe+3].O=P([O-])([O-])OP(=O)([O-])[O-].[Fe+3].O=P([O-])([O-])OP(=O)([O-])[O-].[Fe+3]
Properties
Fe4(P2O7)3
Molar mass 745.224 (anhydrate)
907.348 (nonahydrate)
Appearanceyellow solid (nonahydrate) [1]
insoluble
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Iron(III) pyrophosphate is an inorganic chemical compound with the formula Fe4(P2O7)3.

Contents

Synthesis

Anhydrous iron(III) pyrophosphate can be prepared by heating the mixture of iron(III) metaphosphate and iron(III) phosphate under oxygen with the stoichiometric ratio 1:3. The reactants can be prepared by reacting iron(III) nitrate nonahydrate with phosphoric acid. [2]

It can be also prepared via the following reaction: [3]

3 Na4P2O7(aq) + 4 FeCl3(aq) → Fe4(P2O7)3(s) + 12 NaCl(aq)

Related Research Articles

Electrochemistry Branch of chemistry

Electrochemistry is the branch of physical chemistry concerned with the relationship between electrical potential, as a measurable and quantitative phenomenon, and identifiable chemical change, with either electrical potential as an outcome of a particular chemical change, or vice versa. These reactions involve electrons moving between electrodes via an electronically-conducting phase, separated by an ionically-conducting and electronically insulating electrolyte.

Aqua regia Chemical compound

Aqua regia is a mixture of nitric acid and hydrochloric acid, optimally in a molar ratio of 1:3. Aqua regia is a yellow-orange fuming liquid, so named by alchemists because it can dissolve the noble metals gold and platinum, though not all metals.

Redox Chemical reaction in which oxidation states of atoms are changed

Redox is a type of chemical reaction in which the oxidation states of atoms are changed. Redox reactions are characterized by the actual or formal transfer of electrons between chemical species, most often with one species undergoing oxidation while another species undergoes reduction. The chemical species from which the electron is removed is said to have been oxidized, while the chemical species to which the electron is added is said to have been reduced. In other words:

Iron(III) chloride chemical compound

Iron(III) chloride is the inorganic compound with the formula. Also called ferric chloride, it is a common compound of iron in the +3 oxidation state. The anhydrous compound is a crystalline solid with a melting point of 307.6 °C. The color depends on the viewing angle: by reflected light the crystals appear dark green, but by transmitted light they appear purple-red.

Lead(II) chloride Chemical compound

Lead(II) chloride (PbCl2) is an inorganic compound which is a white solid under ambient conditions. It is poorly soluble in water. Lead(II) chloride is one of the most important lead-based reagents. It also occurs naturally in the form of the mineral cotunnite.

Praseodymium(III) chloride Chemical compound

Praseodymium(III) chloride is the inorganic compound with the formula PrCl3. It is a blue-green solid that rapidly absorbs water on exposure to moist air to form a light green heptahydrate.

Iron(II,III) oxide Chemical compound

Iron(II,III) oxide is the chemical compound with formula Fe3O4. It occurs in nature as the mineral magnetite. It is one of a number of iron oxides, the others being iron(II) oxide (FeO), which is rare, and iron(III) oxide (Fe2O3) which also occurs naturally as the mineral hematite. It contains both Fe2+ and Fe3+ ions and is sometimes formulated as FeO ∙ Fe2O3. This iron oxide is encountered in the laboratory as a black powder. It exhibits permanent magnetism and is ferrimagnetic, but is sometimes incorrectly described as ferromagnetic. Its most extensive use is as a black pigment. For this purpose, it is synthesized rather than being extracted from the naturally occurring mineral as the particle size and shape can be varied by the method of production.

Gold(III) chloride Chemical compound

Gold(III) chloride, traditionally called auric chloride, is a chemical compound of gold and chlorine. With the molecular formula Au2Cl6, the name gold trichloride is a simplification, referring to the empirical formula, AuCl3. The Roman numerals in the name indicate that the gold has an oxidation state of +3, which is common for gold compounds. There is also another related chloride of gold, gold(I) chloride (AuCl). Chloroauric acid, HAuCl4, the product formed when gold dissolves in aqua regia, is sometimes referred to as "gold chloride" or "acid gold trichloride". Gold(III) chloride is very hygroscopic and highly soluble in water as well as ethanol. It decomposes above 160 °C or in light.

Tin(II) chloride Chemical compound

Tin(II) chloride, also known as stannous chloride, is a white crystalline solid with the formula SnCl2. It forms a stable dihydrate, but aqueous solutions tend to undergo hydrolysis, particularly if hot. SnCl2 is widely used as a reducing agent (in acid solution), and in electrolytic baths for tin-plating. Tin(II) chloride should not be confused with the other chloride of tin; tin(IV) chloride or stannic chloride (SnCl4).

Calcium pyrophosphate Chemical compound

Calcium pyrophosphate (Ca2P2O7) is a chemical compound, an insoluble calcium salt containing the pyrophosphate anion. There are a number of forms reported: an anhydrous form, a dihydrate, Ca2P2O7·2H2O and a tetrahydrate, Ca2P2O7·4H2O. Deposition of dihydrate crystals in cartilage are responsible for the severe joint pain in cases of calcium pyrophosphate deposition disease (pseudo gout) whose symptoms are similar to those of gout. Ca2P2O7 is commonly used as a mild abrasive agent in toothpastes, because of its insolubility and nonreactivity toward fluoride.

Ferrate(VI) Ion

Ferrate(VI) is the inorganic anion with the chemical formula [FeO4]2−. It is photosensitive, contributes a pale violet colour to compounds and solutions containing it and is one of the strongest water-stable oxidizing species known. Although it is classified as a weak base, concentrated solutions containing ferrate(VI) are corrosive and attack the skin and are only stable at high pH.

Iron(III) fluoride Chemical compound

Iron(III) fluoride, also known as ferric fluoride, are inorganic compounds with the formula FeF3(H2O)x where x = 0 or 3. They are mainly of interest by researchers, unlike the related iron(III) chlorides. Anhydrous iron(III) fluoride is white, whereas the hydrated forms are light pink.

Iron(III) oxide-hydroxide Chemical compound

Iron(III) oxide-hydroxide or ferric oxyhydroxide is the chemical compound of iron, oxygen, and hydrogen with formula FeO(OH).

iron(II) carbonate, or ferrous carbonate, is a chemical compound with formula FeCO
3
, that occurs naturally as the mineral siderite. At ordinary ambient temperatures, it is a green-brown ionic solid consisting of iron(II) cations Fe2+
and carbonate anions CO2−
3
.

Iron(III) acetate Chemical compound

Ferric acetate is the acetate salt of the coordination complex [Fe3O(OAc)6(H2O)3]+ (OAc is CH3CO2). Commonly the salt is known as "basic iron acetate". The formation of the red-brown complex was once used as a test for ferric ions.

Caesium bromide Chemical compound

Caesium bromide or cesium bromide is an ionic compound of caesium and bromine with the chemical formula CsBr. It is a white or transparent solid with melting point at 636 °C that readily dissolves in water. Its bulk crystals have the cubic CsCl structure, but the structure changes to the rocksalt type in nanometer-thin film grown on mica, LiF, KBr or NaCl substrates.

Iron(III) sulfide, also known as ferric sulfide or sesquisulfide, is one of the three iron sulfides besides FeS and FeS2. It is a solid, black powder but decays at ambient temperature into a yellow-green powder.

Metal halides

Metal halides are compounds between metals and halogens. Some, such as sodium chloride are ionic, while others are covalently bonded. Covalently bonded metal halides may be discrete molecules, such as uranium hexafluoride, or they may form polymeric structures, such as palladium chloride.

Cyclopentadienyliron dicarbonyl dimer Chemical compound

Cyclopentadienyliron dicarbonyl dimer is an organometallic compound with the formula [(η5-C5H5)Fe(CO)2]2, often abbreviated to Cp2Fe2(CO)4, [CpFe(CO)2]2 or even Fp2, with the colloquial name "fip dimer". It is a dark reddish-purple crystalline solid, which is readily soluble in moderately polar organic solvents such as chloroform and pyridine, but less soluble in carbon tetrachloride and carbon disulfide. Cp2Fe2(CO)4 is insoluble in but stable toward water. Cp2Fe2(CO)4 is reasonably stable to storage under air and serves as a convenient starting material for accessing other Fp (CpFe(CO)2) derivatives (described below).

Iron(tetraphenylporphyrinato) chloride Chemical compound

Iron(tetraporphyriinato) chloride is the coordination complex with the formula Fe(TPP)Cl where TPP is the dianion [C44H28N4]2-. The compound is a blue microcrystals that dissolve in chlorinated solvent to give brown solutions. In terms of structure, the complex is five-coordinate with idealized C4v point group symmetry.

References

  1. W.M.Haynes. CRC Handbook of Chemistry and Physics (97th edition). New York: CRC Press, 2016. pp 4-68
  2. Elbouaanani, L.K; Malaman, B; Gérardin, R; Ijjaali, M (2002). "Crystal Structure Refinement and Magnetic Properties of Fe4(P2O7)3 Studied by Neutron Diffraction and Mössbauer Techniques". Journal of Solid State Chemistry. Elsevier BV. 163 (2): 412–420. doi:10.1006/jssc.2001.9415. ISSN   0022-4596.
  3. Rossi L, Velikov KP, Philipse AP (May 2014). "Colloidal iron(III) pyrophosphate particles". Food Chem. 151: 243–7. doi:10.1016/j.foodchem.2013.11.050. PMID   24423528.